ENST00000292408.9:c.1163G>C
MANE Select
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ENSP00000292408.4:p.Gly388Ala
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ENST00000292408.8:c.1163G>C
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ENSP00000292408.4:p.Gly388Ala
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ENST00000393637.5:c.1058-89G>C
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ENSP00000377254.1:n.1058-89G>C
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ENST00000393648.6:c.1097+66G>C
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ENSP00000377259.2:n.1097+66G>C
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ENST00000502906.5:c.1163G>C
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ENSP00000424960.1:p.Gly388Ala
|
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ENST00000508139.1:n.467G>C
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|
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ENST00000511076.1:c.69G>C
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|
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NM_001291980.1:c.1097+66G>C
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NP_001278909.1:n.1097+66G>C
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NM_002011.4:c.1163G>C
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NP_002002.3:p.Gly388Ala
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NM_022963.3:c.1058-89G>C
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NP_075252.2:n.1058-89G>C
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NM_213647.2:c.1163G>C
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NP_998812.1:p.Gly388Ala
|
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XM_005265838.2:c.1163G>C
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XP_005265895.1:p.Gly388Ala
|
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XM_011534464.1:c.1256G>C
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XP_011532766.1:p.Gly419Ala
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XM_011534465.1:c.845G>C
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XP_011532767.1:p.Gly282Ala
|
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XR_941090.1:n.1208G>C
|
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NM_001354984.1:c.1163G>C
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NP_001341913.1:p.Gly388Ala
|
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NM_213647.3:c.1163G>C
MANE Select
|
NP_998812.1:p.Gly388Ala
|
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NM_001291980.2:c.1097+66G>C
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NP_001278909.1:n.1097+66G>C
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NM_001354984.2:c.1163G>C
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NP_001341913.1:p.Gly388Ala
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NM_002011.5:c.1163G>C
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NP_002002.3:p.Gly388Ala
|
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